meddevicedb.com FDA Device Reference

CLEARFIL PHOTO BOND

K872959 Class II Traditional
Decision Date
1987-11-20
Sponsor / Applicant
Kuraray Co.

Technical Specification

510(k) Submission ID K872959
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 1987-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEARFIL PHOTO BOND received FDA 510(k) clearance under submission number K872959, sponsored by Kuraray Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1987-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.